Frontiers in Marine Science,
Journal Year:
2025,
Volume and Issue:
12
Published: May 19, 2025
Antarctic
krill
(
Euphausia
superba
Dana)
is
a
key
species
of
the
Southern
Ocean
ecosystem,
immensely
abundant
and
targeted
by
fishery.
For
their
sustainable
management,
distribution
biomass
estimates
are
required,
typically
achieved
through
acoustic-trawl
surveys.
We
explore
how
environmental
DNA
(eDNA)
can
contribute
to
our
understanding
or
habitat
distribution.
collected
eDNA
samples
filtering
five
liters
seawater
per
sample
in
East
from
surface
(5
m
depth)
seafloor
(381–4422
depth,
total
n
=
110).
used
quantitative
PCR
measure
abundance
age,
metabarcoding
detect
any
species.
This
data
was
compared
acoustic,
visual
trawl
detections
krill.
common
largely
overlapped
with
detections.
Highest
concentrations
were
detected
above
swarms,
declining
increasing
distance
swarms.
Near
recent
sampling
locations,
swarms
more
likely
acoustically
than
near
old
locations.
less
concentrated
continental
slope
area
south
survey
area,
both
for
Both
methods
at
great
depths
(recent
eDNA:
4300
m;
visual:
3080
m).
In
data,
dominant
species,
followed
Thysanoessa
macrura
G.O.
Sars,
which
particularly
larval
stages
throughout
including
swarm
recommend
inclusion
use,
difficult-to-access
areas,
such
as
under
ice
benthic
habitats.
The Science of The Total Environment,
Journal Year:
2023,
Volume and Issue:
873, P. 162322 - 162322
Published: Feb. 18, 2023
Environmental
DNA
(eDNA)
is
the
fastest
growing
biomonitoring
tool
fuelled
by
two
key
features:
time
efficiency
and
sensitivity.
Technological
advancements
allow
rapid
biodiversity
detection
at
both
species
community
levels
with
increasing
accuracy.
Concurrently,
there
has
been
a
global
demand
to
standardise
eDNA
methods,
but
this
only
possible
an
in-depth
overview
of
technological
discussion
pros
cons
available
methods.
We
therefore
conducted
systematic
literature
review
407
peer-reviewed
papers
on
aquatic
published
between
2012
2021.
observed
gradual
increase
in
annual
number
publications
from
four
(2012)
28
(2018),
followed
growth
124
This
was
mirrored
tremendous
diversification
methods
all
aspects
workflow.
For
example,
freezing
applied
preserve
filter
samples,
whereas
we
recorded
12
different
preservation
2021
literature.
Despite
ongoing
standardisation
debate
community,
field
seemingly
moving
fast
opposite
direction
discuss
reasons
implications.
Moreover,
compiling
largest
PCR-primer
database
date,
provide
information
522
141
species-specific
metabarcoding
primers
targeting
wide
range
organisms.
works
as
user-friendly
'distillation'
primer
that
hitherto
scattered
across
hundreds
papers,
list
also
reflects
which
taxa
are
commonly
studied
technology
environments
such
fish
amphibians,
reveals
groups
corals,
plankton
algae
under-studied.
Efforts
improve
sampling
extraction
specificity
reference
databases
crucial
capture
these
ecologically
important
future
surveys.
In
rapidly
diversifying
field,
synthetises
procedures
can
guide
users
towards
best
practice.
Fungal ecology,
Journal Year:
2023,
Volume and Issue:
65, P. 101274 - 101274
Published: July 26, 2023
High
throughput
sequencing
of
PCR
amplicons
derived
from
environmental
DNA
(aka
metabarcoding)
has
become
an
integral
part
fungal
ecology,
enabling
in-depth
characterization
communities.
In
most
cases,
the
rDNA
Internal
Transcribed
Spacer
(ITS)
region,
which
a
long
history
as
target
in
systematics,
is
used
barcode
marker.
Despite
improvements
techniques
and
bioinformatics
approaches,
there
are
inherent
limitations
associated
with
use
single-locus
marker
that
often
ignored.
this
text,
I
discuss
both
biological
methodological
ITS
For
example,
proper
species
delimitation
not
possible
single
marker,
significant
barcoding
gap
(i.e.
interspecific
divergence)
missing
between
sister
taxa
ITS.
Further,
we
can
rarely
be
fully
confident
about
assigned
species-level
taxonomy
based
on
available
reference
sequences.
addition
to
limitations,
extra
layer
complexity
variation
blended
into
metabarcoding
data
due
errors
may
look
similar
natural
molecular
variation.
The
processing
must
take
account
basic
properties
well
generated
biases.
regard,
cannot
adopt
approaches
settings
other
markers,
such
16S
18S,
blindly.
intraspecific
variability
sometimes
intragenomic
variability,
sequences
clustered
approach
level
resolution
community
studies.
Therefore,
argue
concept
amplicon
sequence
variants
(ASVs)
applicable.
Although
region
by
far
best
option
general
(meta)barcoding
for
fungi,
contribution
meant
remind
against
naive
or
simplistic
stimulating
further
discussions.
Molecular Ecology,
Journal Year:
2024,
Volume and Issue:
33(11)
Published: April 16, 2024
Abstract
Molecular
tools
are
an
indispensable
part
of
ecology
and
biodiversity
sciences
implemented
across
all
biomes.
About
a
decade
ago,
the
use
implementation
environmental
DNA
(eDNA)
to
detect
signals
extracted
from
samples
opened
new
avenues
research.
Initial
eDNA
research
focused
on
understanding
population
dynamics
target
species.
Its
scope
thereafter
broadened,
uncovering
previously
unrecorded
via
metabarcoding
in
both
well‐studied
understudied
ecosystems
taxonomic
groups.
The
application
rapidly
became
established
research,
field
by
its
own.
Here,
we
revisit
key
expectations
made
land‐mark
special
issue
Ecology
2012
frame
development
six
areas:
(1)
sample
collection,
(2)
primer
development,
(3)
biomonitoring,
(4)
quantification,
(5)
behaviour
environment
(6)
reference
database
development.
We
pinpoint
success
eDNA,
yet
also
discuss
shortfalls
not
met,
highlighting
areas
priority
identify
unexpected
developments.
In
parallel,
our
retrospective
couples
screening
peer‐reviewed
literature
with
survey
users
including
academics,
end‐users
commercial
providers,
which
address
focus
efforts
advance
eDNA.
With
rapid
ever‐increasing
pace
technical
advances,
future
looks
bright,
successful
applications
best
practices
must
become
more
interdisciplinary
reach
full
potential.
Our
retrospect
gives
towards
concretely
moving
forward.
Molecular Ecology Resources,
Journal Year:
2022,
Volume and Issue:
23(1), P. 174 - 189
Published: Aug. 20, 2022
The
accurate
extraction
of
species-abundance
information
from
DNA-based
data
(metabarcoding,
metagenomics)
could
contribute
usefully
to
diet
analysis
and
food-web
reconstruction,
the
inference
species
interactions,
modelling
population
dynamics
distributions,
biomonitoring
environmental
state
change,
false
positives
negatives.
However,
multiple
sources
bias
noise
in
sampling
processing
combine
inject
error
into
sets.
To
understand
how
extract
abundance
information,
it
is
useful
distinguish
two
concepts.
(i)
Within-sample
across-species
quantification
describes
relative
abundances
one
sample.
(ii)
Across-sample
within-species
each
individual
varies
sample
sample,
such
as
over
a
time
series,
an
gradient
or
different
experimental
treatments.
First,
we
review
literature
on
methods
recover
(by
removing
what
call
"species
pipeline
biases")
"pipeline
noise").
We
argue
that
many
ecological
questions
can
be
answered
with
just
quantification,
therefore
demonstrate
use
"DNA
spike-in"
correct
for
information.
also
introduce
model-based
estimator
used
sets
without
physical
spike-in
approximate
noise.
Methods in Ecology and Evolution,
Journal Year:
2023,
Volume and Issue:
14(4), P. 1130 - 1146
Published: Feb. 13, 2023
1:
Metabarcoding
(high-throughput
sequencing
of
marker
gene
amplicons)
has
emerged
as
a
promising
and
cost-effective
method
for
characterizing
insect
community
samples.
Yet,
the
methodology
varies
greatly
among
studies
its
performance
not
been
systematically
evaluated
to
date.
In
particular,
it
is
unclear
how
accurately
metabarcoding
can
resolve
species
communities
in
terms
presence-absence,
abundances,
biomass.
2:
Here
we
use
mock
experiments
simple
probabilistic
model
evaluate
effect
different
DNA
extraction
protocols
on
performance.
Specifically,
ask
four
questions:
(Q1)
How
consistent
are
recovered
profiles
across
replicate
communities?;
(Q2)
does
choice
lysis
buffer
affect
recovery
original
community?;
(Q3)
estimates
affected
by
differing
times
homogenization?;
(Q4)
Is
possible
obtain
adequate
abundance
through
biological
spike-ins?
3:
We
show
that
quite
variable
replicates.
general,
mild
protocol
better
at
reconstructing
lists
approximate
counts,
while
homogenization
retrieving
biomass
composition.
Small
insects
more
likely
be
detected
lysates,
some
tough
require
detected.
Results
less
replicates
lysates
than
homogenates.
Some
associated
with
strong
PCR
amplification
bias,
which
complicates
reconstruction
counts.
spike-in
data,
determined
roughly
40%
standard
error
homogenates,
50%
under
ideal
conditions.
latter
case,
however,
this
often
requires
species-specific
reference
data
generalizes
4:
conclude
non-destructive,
approach
shows
highest
promise
presence/absence
description
community,
also
allowing
future
morphological
or
molecular
work
material.
However,
perform
composition,
particular
Philosophical Transactions of the Royal Society B Biological Sciences,
Journal Year:
2024,
Volume and Issue:
379(1904)
Published: May 5, 2024
Holistic
insect
monitoring
needs
scalable
techniques
to
overcome
taxon
biases,
determine
species
abundances,
and
gather
functional
traits
for
all
species.
This
requires
that
we
address
taxonomic
impediments
the
paucity
of
data
on
abundance,
biomass
traits.
We
here
outline
how
these
deficiencies
could
be
addressed
at
scale.
The
workflow
starts
with
large-scale
barcoding
(megabarcoding)
specimens
from
mass
samples
obtained
biomonitoring
sites.
barcodes
are
then
used
group
into
molecular
operational
units
subsequently
tested/validated
as
a
second
source
(e.g.
morphology).
New
described
using
barcodes,
images
short
diagnoses,
abundance
collected
both
new
specimen
discovery
become
raw
material
training
artificial
intelligence
identification
algorithms
collecting
trait
such
body
size,
feeding
modes.
Additional
can
vouchers
by
genomic
tools
developed
ecologists.
Applying
this
pipeline
few
per
site
will
lead
greatly
improved
regardless
whether
composition
sample
is
determined
images,
metabarcoding
or
megabarcoding.
article
part
theme
issue
'Towards
toolkit
global
biodiversity
monitoring'.
Methods in Ecology and Evolution,
Journal Year:
2024,
Volume and Issue:
15(5), P. 806 - 815
Published: March 27, 2024
Abstract
Ecological
and
ecosystem
monitoring
is
rapidly
shifting
towards
using
environmental
DNA
(eDNA)
data,
particularly
in
aquatic
systems.
This
approach
enables
a
combined
coverage
of
biodiversity
across
all
major
organismal
groups
the
assessment
ecological
indices.
Yet,
most
current
approaches
are
not
exploiting
full
potential
eDNA
largely
interpreting
results
localized
perspective.
In
riverine
networks,
by
explicitly
modelling
hydrological
transport
associated
decay,
hydrology‐based
models
enable
upscaling
eDNA‐based
diversity
information,
providing
spatially
integrated
inference.
To
capitalize
on
these
unprecedented
data
translate
it
into
space‐filling
projections,
streamlined
implementation
needed.
Here,
we
introduce
eDITH
R‐package,
implementing
model
to
project
networks
with
minimal
prior
information.
couples
species
distribution
relating
local
taxon's
shedding
rate
streamwater
covariates,
mass
balance
expressing
concentration
at
river's
cross‐section
as
weighted
sum
upstream
contributions,
an
observational
accounting
for
uncertainties
measurements.
By
leveraging
replicated
measurements
hydro‐morphological
disentangling
various
sources,
produces
maps
spatial
any
chosen
resolution.
applicable
both
metabarcoding
taxon
whose
can
be
retrieved
streamwater.
The
package
provides
user‐friendly
functions
single‐run
execution
fitting
Bayesian
methods
(via
BayesianTools
package)
non‐linear
optimization.
An
interface
DHARMa
allows
validation
via
posterior
predictive
checks.
Necessary
preliminary
steps
such
watershed
delineation
characterization
implemented
rivnet
package.
We
illustrate
's
workflow
functionalities
two
case
studies
from
published
fish
data.
eDITH,
specifically
intended
ecologists
conservation
biologists.
It
used
without
previous
knowledge
but
also
customization
experienced
users.
Ultimately,
river
globally,
transforming
how
state
change
systems
tracked
high
resolution
highly
versatile
manner.